TW201413763A - Laminated ceramic capacitor and production method for laminated ceramic capacitor - Google Patents

Laminated ceramic capacitor and production method for laminated ceramic capacitor Download PDF

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TW201413763A
TW201413763A TW102127661A TW102127661A TW201413763A TW 201413763 A TW201413763 A TW 201413763A TW 102127661 A TW102127661 A TW 102127661A TW 102127661 A TW102127661 A TW 102127661A TW 201413763 A TW201413763 A TW 201413763A
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ceramic
ratio
internal electrode
dielectric layer
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TWI470659B (en
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Shinichi Yamaguchi
Shoichiro Suzuki
Akitaka Doi
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Murata Manufacturing Co
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G4/00Fixed capacitors; Processes of their manufacture
    • H01G4/002Details
    • H01G4/005Electrodes
    • H01G4/008Selection of materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G13/00Apparatus specially adapted for manufacturing capacitors; Processes specially adapted for manufacturing capacitors not provided for in groups H01G4/00 - H01G11/00
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G4/00Fixed capacitors; Processes of their manufacture
    • H01G4/002Details
    • H01G4/005Electrodes
    • H01G4/008Selection of materials
    • H01G4/0085Fried electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G4/00Fixed capacitors; Processes of their manufacture
    • H01G4/002Details
    • H01G4/005Electrodes
    • H01G4/012Form of non-self-supporting electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G4/00Fixed capacitors; Processes of their manufacture
    • H01G4/002Details
    • H01G4/018Dielectrics
    • H01G4/06Solid dielectrics
    • H01G4/08Inorganic dielectrics
    • H01G4/12Ceramic dielectrics
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G4/00Fixed capacitors; Processes of their manufacture
    • H01G4/30Stacked capacitors

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  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Ceramic Capacitors (AREA)
  • Fixed Capacitors And Capacitor Manufacturing Machines (AREA)

Abstract

Provided is a laminated ceramic capacitor having thinner ceramic dielectric layers and exhibiting excellent durability and good dielectric characteristics even when a high electric field strength voltage is applied thereto. The laminated ceramic capacitor comprises: a ceramic laminate (5) having a plurality of ceramic dielectric layers (2) laminated therein; a plurality of internal electrodes (3, 4) arranged inside the ceramic laminate (5) so as to face each other having the ceramic dielectric layers (2) therebetween; and external electrodes (6, 7) arranged on the outside surface of the ceramic laminate so as to be electrically connected to the internal electrodes. The internal electrodes contain Ni and Sn and the laminated ceramic capacitor is configured so as to fulfill the conditions that at least 75% of an area in the internal electrodes having a depth of 20 nm from the surface facing the ceramic dielectric layers has a Sn/(Ni+Sn) ratio of at least 0.001 by molar ratio, and less than 40% of the area in a center area in the thickness direction of the internal electrodes has an Sn/(Ni+Sn) ratio of at least 0.001 by molar ratio.

Description

積層陶瓷電容器及積層陶瓷電容器之製造方法 Method for manufacturing laminated ceramic capacitor and laminated ceramic capacitor

本發明係關於一種積層陶瓷電容器及積層陶瓷電容器之製造方法。 The present invention relates to a method of manufacturing a multilayer ceramic capacitor and a multilayer ceramic capacitor.

近年來,伴隨著電子裝置技術之發展,要求積層陶瓷電容器小型化及大電容化。為了滿足該等要求,而不斷推進構成積層陶瓷電容器之陶瓷介電層之薄層化。然而,若使陶瓷介電層薄層化,則施加至每一層之電場強度會相對提高。由此,要求提高電壓施加時之耐久性、可靠性。 In recent years, with the development of electronic device technology, it is required to reduce the size and capacitance of laminated ceramic capacitors. In order to satisfy these requirements, the thinning of the ceramic dielectric layer constituting the laminated ceramic capacitor is continuously advanced. However, if the ceramic dielectric layer is thinned, the electric field strength applied to each layer will be relatively increased. Therefore, it is required to improve the durability and reliability at the time of voltage application.

作為積層陶瓷電容器,已知有例如包括積層體與複數個外部電極之積層陶瓷電容器,該積層體包含所積層之複數個陶瓷介電層、及沿著陶瓷介電層間之界面而形成之複數個內部電極,該複數個外部電極係形成於積層體之外表面且與內部電極電性連接(參照專利文獻1)。而且,於該專利文獻1之積層陶瓷電容器中,作為內部電極,揭示有使用Ni作為主成分者。 As a multilayer ceramic capacitor, for example, a multilayer ceramic capacitor including a laminate and a plurality of external electrodes is known, and the laminate includes a plurality of ceramic dielectric layers stacked and a plurality of layers formed along an interface between the ceramic dielectric layers. The internal electrode is formed on the outer surface of the laminated body and electrically connected to the internal electrode (see Patent Document 1). Further, in the multilayer ceramic capacitor of Patent Document 1, as the internal electrode, those using Ni as a main component are disclosed.

先前技術文獻 Prior technical literature 專利文獻 Patent literature

專利文獻1:日本專利特開平11-283867號公報 Patent Document 1: Japanese Patent Laid-Open No. Hei 11-283867

然而,於具備使用Ni作為主成分之內部電極之上述專利文獻1之 積層陶瓷電容器中,存在如下問題:為了應對近年來之小型化及大電容化之要求,高電壓施加時之耐久性尚不充分。 However, in the above Patent Document 1 having an internal electrode using Ni as a main component In the multilayer ceramic capacitor, there is a problem in that durability in the application of high voltage is not sufficient in order to meet the demands of miniaturization and large capacitance in recent years.

本發明係為了解決上述問題而完成者,其目的在於提供一種積層陶瓷電容器,該積層陶瓷電容器之陶瓷介電層更薄層化,且即便於施加有高電場強度之電壓之情形時,亦顯示優異之耐久性與良好之介電特性。 The present invention has been made to solve the above problems, and an object thereof is to provide a multilayer ceramic capacitor in which a ceramic dielectric layer is thinner and exhibits even when a voltage having a high electric field strength is applied. Excellent durability and good dielectric properties.

為了解決上述問題,本發明之積層陶瓷電容器之特徵在於包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;且上述內部電極含有Ni與Sn,並且,上述內部電極之自與上述陶瓷介電層對向之表面起深度為20nm之區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上,且,上述內部電極之厚度方向之中央區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%。 In order to solve the above problems, the multilayer ceramic capacitor of the present invention is characterized by comprising: a ceramic laminate which is formed by laminating a plurality of ceramic dielectric layers; and a plurality of internal electrodes which are interconnected by the ceramic dielectric layer And the external electrode is disposed on the outer surface of the ceramic laminate, and the internal electrode includes Ni and Sn, and the external electrode is disposed inside the ceramic laminate; and The Sn/(Ni+Sn) ratio in the region of the internal electrode from the surface opposite to the ceramic dielectric layer to the surface of the depth of 20 nm with respect to the sum of Sn and Ni is 0.001 in terms of the molar ratio. The ratio of the above region is 75% or more, and the ratio of Sn in the central region in the thickness direction of the internal electrode to the total amount of Sn and Ni, that is, the Sn/(Ni+Sn) ratio is 0.001 in terms of the molar ratio. The proportion of the above regions is less than 40%.

又,本發明之積層陶瓷電容器之製造方法之特徵在於:其係製造如下積層陶瓷電容器之方法,該積層陶瓷電容器包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;且 上述內部電極含有Ni與Sn,並且,上述內部電極之自與上述陶瓷介電層對向之表面起深度為20nm之區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上,且,上述內部電極之厚度方向之中央區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%;上述積層陶瓷電容器之製造方法包括如下步驟:形成未煅燒陶瓷積層體,該未煅燒陶瓷積層體具有於積層並煅燒後成為上述陶瓷介電層之複數個未煅燒陶瓷介電層、及藉由塗佈導電膏而形成且沿著上述未煅燒陶瓷介電層間之複數個界面配設之複數個未煅燒內部電極圖案;以及藉由對上述未煅燒陶瓷積層體進行煅燒而獲得上述陶瓷積層體;並且,作為上述導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有與構成上述未煅燒陶瓷介電層之陶瓷材料粉末相同之組成或以其為基準之組成的陶瓷材料粉末中調配Sn成分而成。 Further, a method of manufacturing a multilayer ceramic capacitor of the present invention is characterized in that it is a method of manufacturing a laminated ceramic capacitor comprising: a ceramic laminate in which a plurality of ceramic dielectric layers are laminated; and a plurality of internal layers And an electrode disposed inside the ceramic laminate in such a manner as to face each other with the ceramic dielectric layer interposed therebetween; and an external electrode disposed in the ceramic laminate in a manner to be electrically connected to the internal electrode Outside surface; and The internal electrode contains Ni and Sn, and the ratio of Sn in a region having a depth of 20 nm from the surface facing the ceramic dielectric layer to the total amount of Sn and Ni is Sn/(Ni+). The ratio of Sn to the region of 0.001 or more in terms of the molar ratio is 75% or more, and the ratio of Sn in the central region in the thickness direction of the internal electrode to the total amount of Sn and Ni is Sn/(Ni+ The ratio of Sn) to the region of 0.001 or more in terms of the molar ratio is less than 40%; the manufacturing method of the above laminated ceramic capacitor includes the steps of: forming an uncalcined ceramic laminate having a layer and calcining a plurality of uncalcined ceramic dielectric layers forming the ceramic dielectric layer; and a plurality of uncalcined internal electrode patterns formed by coating a conductive paste and disposed along a plurality of interfaces between the uncalcined ceramic dielectric layers; And obtaining the ceramic laminate by firing the uncalcined ceramic laminate; and, as the conductive paste, using a conductive paste containing the same material and containing the Sn component, the Sn component is blended with the same material to have The calcined powder is not the same as the ceramic dielectric layer of a ceramic material or in the above reference of a ceramic material powder consisting of Sn component formulated together.

再者,於本發明中,所謂導電膏中所含有之Sn成分調配相同材料係指於與構成未煅燒陶瓷介電層之陶瓷材料粉末(介電層用陶瓷材料粉末)相同之陶瓷材料粉末、或與介電層用陶瓷材料粉末之組成相同之陶瓷材料粉末、進而具有類似於介電層用陶瓷材料粉末之組成之陶瓷材料粉末等材料中調配例如SnO2之類的Sn化合物而成之材料之廣義概念。 In the present invention, the composition of the Sn component contained in the conductive paste is the same as the ceramic material powder (the ceramic material powder for the dielectric layer) constituting the uncalcined ceramic dielectric layer, Or a material obtained by blending a ceramic material powder having the same composition as that of the ceramic material powder for the dielectric layer, and further having a Sn compound such as SnO 2 in a material such as a ceramic material powder having a composition similar to the ceramic material powder for the dielectric layer. The broad concept.

又,本發明之另一積層陶瓷電容器之特徵在於包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷 積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;且上述內部電極含有Ni與Sn,並且Sn固溶於Ni,上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例為2原子%以上,且,上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例較上述內部電極之自與上述陶瓷介電層之界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上。 Further, another multilayer ceramic capacitor of the present invention is characterized by comprising: a ceramic laminate which is formed by laminating a plurality of ceramic dielectric layers; and a plurality of internal electrodes which are mutually opposed to each other by interposing the ceramic dielectric layers Arranged to the above ceramics An internal electrode; and an external electrode disposed on the outer surface of the ceramic laminate in a manner to be electrically connected to the internal electrode; and the internal electrode contains Ni and Sn, and Sn is dissolved in Ni, and the internal electrode is a ratio of Sn to a total amount of Sn and Ni in a region having a depth of 2 nm from an interface with the ceramic dielectric layer of 2 atom% or more, and an internal electrode from an interface with the ceramic dielectric layer The ratio of Sn in a region having a depth of 2 nm to the total amount of Sn and Ni is 1.0 atom% or more larger than the ratio of Sn in a region having a depth of 20 nm or more from the interface with the ceramic dielectric layer.

又,本發明之另一積層陶瓷電容器之製造方法之特徵在於:該積層陶瓷電容器包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;上述內部電極含有Ni與Sn,且Sn固溶於Ni;上述積層陶瓷電容器之製造方法包括如下步驟:形成未煅燒陶瓷積層體,該未煅燒陶瓷積層體具有於積層並煅燒後成為上述陶瓷介電層之複數個未煅燒陶瓷介電層、及藉由塗佈導電膏而形成且沿著上述未煅燒陶瓷介電層間之複數個界面配設之複數個未煅燒內部電極圖案;以及藉由對上述未煅燒陶瓷積層體進行煅燒而獲得上述陶瓷積層體;且作為上述導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有含有構成陶瓷材料粉末之至少一部分元素之組成的陶瓷材料粉末中調配Sn成分而成,上述陶瓷材料粉末構成上述未煅燒陶瓷介電層,並且, 以藉由對上述未煅燒陶瓷積層體進行煅燒而獲得上述陶瓷積層體之方式構成,上述陶瓷積層體係構成上述陶瓷積層體之上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例為2原子%以上,且上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例較上述內部電極之自與上述陶瓷介電層之界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上。 Further, a method of manufacturing another multilayer ceramic capacitor of the present invention is characterized in that the multilayer ceramic capacitor comprises: a ceramic laminate in which a plurality of ceramic dielectric layers are laminated; and a plurality of internal electrodes are separated by a plurality of layers. The ceramic dielectric layer is disposed opposite to each other in the ceramic laminate; and the external electrode is disposed on the outer surface of the ceramic laminate in a manner to be electrically connected to the internal electrode; and the internal electrode includes Ni and Sn, and Sn is solid-solubilized in Ni; the manufacturing method of the above laminated ceramic capacitor includes the steps of: forming an uncalcined ceramic laminate having a plurality of layers of the ceramic dielectric layer after lamination and calcination An uncalcined ceramic dielectric layer, and a plurality of uncalcined internal electrode patterns formed by coating a conductive paste and disposed along a plurality of interfaces between the unfired ceramic dielectric layers; and laminating the uncalcined ceramics The body is calcined to obtain the ceramic laminate; and as the conductive paste, a conductive paste containing the same material is used, and the Sn is formed. Formulation-based material having the same ceramic material powder contains at least a part of elements constituting the ceramic material powder consisting of Sn component formulated together, the ceramic material powder constituting the unfired ceramic dielectric layers, and, The ceramic laminate is obtained by calcining the unfired ceramic laminate, and the ceramic laminate system comprises the internal electrode of the ceramic laminate having a depth of 2 nm from an interface with the ceramic dielectric layer. The ratio of Sn in the region to the total amount of Sn and Ni is 2 atom% or more, and the total of Sn in the region of the internal electrode from the interface with the ceramic dielectric layer at a depth of 2 nm with respect to Sn and Ni The ratio of the amount is 1.0 atom% or more larger than the ratio of Sn in a region having a depth of 20 nm or more from the interface with the ceramic dielectric layer.

本發明之積層陶瓷電容器由於滿足如下要件,即,內部電極含有Ni與Sn,並且內部電極之自與陶瓷介電層對向之表面起深度為20nm之區域(界面附近區域)內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上,且內部電極之厚度方向之中央區域(電極內部區域)內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%,故而可獲得如下積層陶瓷電容器:能夠獲得高靜電電容,且高溫負荷壽命優異、可靠性高。 The multilayer ceramic capacitor of the present invention satisfies the requirement that the internal electrode contains Ni and Sn, and the internal electrode is Sn/(in a region having a depth of 20 nm from the surface opposite to the ceramic dielectric layer (in the vicinity of the interface). The ratio of Ni+Sn) to the region of 0.001 or more in terms of the molar ratio is 75% or more, and the Sn/(Ni+Sn) ratio in the central region (electrode inner region) of the thickness direction of the internal electrode is in the molar ratio. Since the ratio of the region of 0.001 or more is less than 40%, the following multilayer ceramic capacitor can be obtained: high electrostatic capacitance can be obtained, high-temperature load life is excellent, and reliability is high.

即,於本發明中,藉由使內部電極Ni-Sn合金化而使陶瓷介電層與內部電極之界面之狀態產生變化,認為該情況有助於高溫負荷壽命之提高。尤其是,推測在內部電極之與陶瓷介電層之界面附近區域存在大量Ni-Sn合金時對高溫負荷壽命之提高而言發揮重要作用。 That is, in the present invention, the state of the interface between the ceramic dielectric layer and the internal electrode is changed by alloying the internal electrode Ni-Sn, and this is considered to contribute to an improvement in the high-temperature load life. In particular, it is presumed that the presence of a large amount of Ni-Sn alloy in the vicinity of the interface between the internal electrode and the ceramic dielectric layer plays an important role in improving the high-temperature load life.

另一方面,內部電極之厚度方向之中央區域(電極內部區域)由於對高溫負荷壽命之提高並無特別幫助,故可不必大量存在Ni-Sn合金。 On the other hand, the central region (electrode inner region) in the thickness direction of the internal electrode does not particularly contribute to the improvement of the high-temperature load life, so that it is not necessary to have a large amount of the Ni-Sn alloy.

再者,藉由使Sn於內部電極之界面附近區域以高於電極內部區域之機率存在而可獲得高靜電電容之理由雖然不一定明確,但推測其原因在於:藉由使Sn在內部電極之界面附近區域與電極內部區域內存在之比例不同(Sn於界面附近區域以高於電極內部區域之機率存在), 而在界面附近區域與電極內部區域中,晶格之晶格常數產生差,從而在積層陶瓷電容器內部殘留應力之分佈狀態產生變化。 Further, the reason why a high electrostatic capacitance can be obtained by making Sn in the vicinity of the interface of the internal electrode higher than the internal region of the electrode is not necessarily clear, but it is presumed that the reason is that Sn is made at the internal electrode. The ratio between the area near the interface and the inner area of the electrode is different (Sn exists in the vicinity of the interface at a higher probability than the inner area of the electrode), On the other hand, in the region near the interface and the inner region of the electrode, the lattice constant of the crystal lattice is inferior, and the distribution state of the residual stress inside the multilayer ceramic capacitor changes.

又,本發明之積層陶瓷電容器之製造方法包括如下步驟:形成未煅燒陶瓷積層體,該未煅燒陶瓷積層體具有複數個未煅燒陶瓷介電層、及藉由塗佈導電膏而形成且沿著未煅燒陶瓷介電層間之複數個界面配設之複數個未煅燒之內部電極圖案;以及藉由對未煅燒陶瓷積層體進行煅燒而獲得陶瓷積層體;並且,作為導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有與構成未煅燒陶瓷介電層之陶瓷材料粉末相同之組成或以其為基準之組成的陶瓷材料粉末中調配Sn成分而成,故而可確實地製造具備如下構成、能夠獲得大的靜電電容、高溫負荷壽命優異且可靠性高之積層陶瓷電容器,上述構成係內部電極之自與陶瓷介電層對向之表面起深度為20nm之區域(界面附近區域)內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上,且內部電極之厚度方向之中央區域(電極內部區域)內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%之構成,即,Sn在內部電極之界面附近區域以高於電極內部區域之機率存在之構成。 Moreover, the manufacturing method of the multilayer ceramic capacitor of the present invention comprises the steps of: forming an uncalcined ceramic laminate having a plurality of uncalcined ceramic dielectric layers, and formed by coating a conductive paste and along a plurality of uncalcined internal electrode patterns disposed at a plurality of interfaces between the uncalcined ceramic dielectric layers; and a ceramic laminate obtained by calcining the uncalcined ceramic laminate; and, as a conductive paste, using a Sn-containing composition a conductive paste of the same material, the Sn component is formulated with the same material in a ceramic material powder having the same composition as or composed of the ceramic material powder constituting the uncalcined ceramic dielectric layer, and thus the Sn component is blended. A multilayer ceramic capacitor having the following configuration, capable of obtaining a large electrostatic capacitance, excellent high-temperature load life, and high reliability, wherein the internal electrode of the above-described structure has a depth of 20 nm from the surface facing the ceramic dielectric layer ( The ratio of Sn/(Ni+Sn) in the region near the interface to the region of 0.001 or more in terms of the molar ratio is 75% or more, and The ratio of Sn/(Ni+Sn) in the central region (electrode inner region) in the thickness direction of the electrode to the region of 0.001 or more in terms of the molar ratio is less than 40%, that is, Sn is near the interface of the internal electrode. The region is constructed with a higher probability than the inner region of the electrode.

於本發明之積層陶瓷電容器之製造方法中,如上所述,作為導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有與構成未煅燒陶瓷介電層之陶瓷材料粉末相同之組成或以其為基準之組成的陶瓷材料粉末中調配Sn成分而成,因此,於煅燒步驟中,相同材料(Sn成分調配相同材料)被牽引至親和性較高之陶瓷介電層側,並且相同材料中所調配之Sn成分亦被牽引至陶瓷介電層側。其結果,可確實地、並且高效地製造具備如下特有之構成之積層陶瓷電容器,即,相較於內部電極之內部(電極內部區域),Sn在與陶瓷介電層之界面(界面附近區域)中以更高之機率存在。 In the method for producing a multilayer ceramic capacitor of the present invention, as described above, as the conductive paste, a conductive paste containing the same material as the Sn component is used, and the Sn component is formulated with the same material as the ceramic having the dielectric layer constituting the uncalcined ceramic. The ceramic material powder having the same composition of the material powder or the composition thereof is formulated with the Sn component. Therefore, in the calcination step, the same material (the Sn component is blended with the same material) is pulled to the ceramic dielectric having higher affinity. The layer side, and the Sn component formulated in the same material is also pulled to the ceramic dielectric layer side. As a result, it is possible to reliably and efficiently manufacture a multilayer ceramic capacitor having a specific structure in which Sn is in the interface with the ceramic dielectric layer (in the vicinity of the interface) compared to the inside of the internal electrode (electrode inner region). There is a higher chance of being in the middle.

又,本發明之另一積層陶瓷電容器係以如下方式構成,即,內部電極含有Ni與Sn,並且Sn固溶於Ni,內部電極之自與陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例為2原子%以上,且內部電極之自與陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例較自與陶瓷介電層之界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上,因此,可提供能夠獲得高靜電電容、高溫負荷壽命優異且可靠性高之積層陶瓷電容器。 Further, another multilayer ceramic capacitor of the present invention is configured such that the internal electrode contains Ni and Sn, and Sn is dissolved in Ni, and the internal electrode has a depth of 2 nm from the interface with the ceramic dielectric layer. The ratio of Sn to the total amount of Sn and Ni is 2 atom% or more, and the ratio of Sn in the region of the internal electrode from the interface with the ceramic dielectric layer to the depth of 2 nm is proportional to the total amount of Sn and Ni. Since the ratio of Sn in the region having a depth of 20 nm or more from the interface with the ceramic dielectric layer is 1.0 atom% or more, it is possible to provide a multilayer ceramic capacitor which is capable of obtaining high electrostatic capacitance, high temperature load life, and high reliability.

於本發明之另一積層陶瓷電容器中,認為內部電極Ni-Sn合金化,且Sn之比例具備上述要件,藉此陶瓷介電層與內部電極之界面之狀態產生變化,藉由該情況使高溫負荷壽命提高。尤其是,推測在內部電極之自與陶瓷介電層之界面起深度為2nm之區域存在大量Ni-Sn合金時對高溫負荷壽命之提高而言發揮重要作用。 In another multilayer ceramic capacitor of the present invention, it is considered that the internal electrode Ni-Sn is alloyed, and the ratio of Sn has the above-described requirements, whereby the state of the interface between the ceramic dielectric layer and the internal electrode changes, and the temperature is high by the situation. Increased load life. In particular, it is presumed that the presence of a large amount of Ni-Sn alloy in a region having a depth of 2 nm from the interface with the ceramic dielectric layer plays an important role in improving the high-temperature load life.

另一方面,內部電極之自與陶瓷介電層之界面起深度為20nm以上之區域由於對高溫負荷壽命之提高並無特別幫助,故可不必大量存在Ni-Sn合金。 On the other hand, the region of the internal electrode from the interface with the ceramic dielectric layer having a depth of 20 nm or more does not particularly contribute to the improvement of the high-temperature load life, so that it is not necessary to have a large amount of the Ni-Sn alloy.

又,於本發明之積層陶瓷電容器之製造方法中,如上所述,作為導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有含有構成陶瓷材料粉末之至少一部分元素之組成的陶瓷材料粉末中調配Sn成分而成,上述陶瓷材料粉末構成未煅燒陶瓷介電層,並且藉由對未煅燒陶瓷積層體進行煅燒,而可獲得如下陶瓷積層體,即,構成陶瓷積層體之內部電極之自與陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例為2原子%以上,且內部電極之自與陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例較自與陶瓷介電層之界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上,從而於煅燒步驟中, 相同材料(Sn成分調配相同材料)被牽引至親和性較高之陶瓷介電層側,並且相同材料中所調配之Sn成分亦被牽引至陶瓷介電層側,因此,可確實地獲得內部電極之自與陶瓷介電層之界面起深度為2nm之區域內之Sn之比例為2原子%以上、且自界面起深度為2nm之區域內之Sn之比例較自上述界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上的陶瓷積層體,且可高效地製造能夠獲得高靜電電容、高溫負荷壽命優異且可靠性高之積層陶瓷電容器。 Further, in the method for producing a multilayer ceramic capacitor of the present invention, as described above, a conductive paste containing the same material as the Sn component is used as the conductive paste, and the Sn component is blended with the same material to have at least a part of the powder containing the constituent ceramic material. The ceramic material powder having the composition of the elements is prepared by blending a Sn material, and the ceramic material powder constitutes an uncalcined ceramic dielectric layer, and by calcining the uncalcined ceramic laminate, the following ceramic laminate can be obtained, that is, the ceramic is formed. The ratio of Sn in a region having a depth of 2 nm from the interface with the ceramic dielectric layer to the total amount of Sn and Ni in the internal electrode of the laminate is 2 atom% or more, and the internal electrode is self- and ceramic dielectric layer The ratio of Sn in the region having a depth of 2 nm to the total amount of Sn and Ni is 1.0 atom% or more larger than the ratio of Sn in a region having a depth of 20 nm or more from the interface with the ceramic dielectric layer, thereby calcining In the step, The same material (the Sn composition is blended with the same material) is pulled to the ceramic dielectric layer side with higher affinity, and the Sn component blended in the same material is also pulled to the ceramic dielectric layer side, so that the internal electrode can be surely obtained. The ratio of Sn in a region having a depth of 2 nm from the interface with the ceramic dielectric layer is 2 atom% or more, and the ratio of Sn in a region having a depth of 2 nm from the interface is 20 nm or more from the interface. A ceramic laminate having a ratio of Sn in the region of 1.0 at% or more is high, and a multilayer ceramic capacitor which can obtain a high electrostatic capacitance, has a high temperature load life, and is highly reliable can be efficiently produced.

1‧‧‧積層陶瓷電容器 1‧‧‧Multilayer ceramic capacitors

2‧‧‧陶瓷介電層 2‧‧‧Ceramic dielectric layer

3、4‧‧‧內部電極 3, 4‧‧‧ internal electrodes

5‧‧‧陶瓷積層體 5‧‧‧Ceramic laminate

6、7‧‧‧外部電極 6, 7‧‧‧ external electrodes

8‧‧‧上部區域 8‧‧‧ upper area

9‧‧‧中央區域 9‧‧‧Central area

10‧‧‧下部區域 10‧‧‧ Lower area

L‧‧‧長度 L‧‧‧ length

T‧‧‧厚度 T‧‧‧ thickness

W‧‧‧寬度 W‧‧‧Width

圖1係表示本發明之實施形態之積層陶瓷電容器之構成的前視剖面圖。 Fig. 1 is a front cross-sectional view showing the configuration of a multilayer ceramic capacitor according to an embodiment of the present invention.

圖2係表示對構成本發明之實施形態之積層陶瓷電容器之內部電極進行利用WDX之Ni與Sn之映射分析之部位的說明圖。 FIG. 2 is an explanatory view showing a portion where the internal electrodes constituting the multilayer ceramic capacitor of the embodiment of the present invention are subjected to mapping analysis of Ni and Sn by WDX.

圖3係表示藉由WDX對構成本發明之實施形態之積層陶瓷電容器之內部電極進行Ni之映射分析所得之結果的圖。 Fig. 3 is a view showing a result of mapping analysis of Ni by internal electrodes constituting the multilayer ceramic capacitor of the embodiment of the present invention by WDX.

圖4係表示藉由WDX對構成本發明之實施形態之積層陶瓷電容器之內部電極進行Sn之映射分析所得之結果的圖。 Fig. 4 is a view showing a result of mapping analysis of Sn by internal electrodes constituting the multilayer ceramic capacitor of the embodiment of the present invention by WDX.

圖5係表示構成本發明之另一實施形態之積層陶瓷電容器之陶瓷介電層與內部電極的界面附近之Sn之STEM-EDX映像之圖。 Fig. 5 is a view showing a STEM-EDX image of Sn in the vicinity of the interface between the ceramic dielectric layer and the internal electrode of the multilayer ceramic capacitor according to another embodiment of the present invention.

以下表示本發明之實施形態,對設為本發明之特徵之部分進行更詳細之說明。 The embodiments of the present invention are shown below, and the features which are characteristic of the present invention will be described in more detail.

[實施形態1] [Embodiment 1] <積層陶瓷電容器之構成> <Composition of laminated ceramic capacitors>

圖1係表示本發明之一實施形態(實施形態1)之積層陶瓷電容器之構成的前視剖面圖。 Fig. 1 is a front cross-sectional view showing the configuration of a multilayer ceramic capacitor according to an embodiment (Embodiment 1) of the present invention.

該積層陶瓷電容器1具備陶瓷積層體5。陶瓷積層體5包括所積層 之複數個陶瓷介電層2、及以介隔陶瓷介電層2而互相對向之方式配設於其內部之複數個內部電極3、4。再者,配設於陶瓷介電層2之內部之內部電極3、4係交替地引出至陶瓷積層體5之相反側之端面。 This multilayer ceramic capacitor 1 is provided with a ceramic laminate 5 . The ceramic laminate 5 includes a layer The plurality of ceramic dielectric layers 2 and the plurality of internal electrodes 3 and 4 disposed inside the ceramic dielectric layer 2 so as to oppose each other. Further, the internal electrodes 3 and 4 disposed inside the ceramic dielectric layer 2 are alternately drawn to the end faces on the opposite sides of the ceramic laminate 5 .

而且,於陶瓷積層體5之互相對向之端面,以與內部電極3、4電性連接之方式配設有外部電極6、7。 Further, external electrodes 6 and 7 are disposed on the end faces of the ceramic laminate 5 facing each other so as to be electrically connected to the internal electrodes 3 and 4.

於陶瓷積層體5之外表面上之互相對向之端面形成有外部電極6、7。而且,外部電極6、7分別與交替地被引出至相反側之端面之內部電極3、4連接。 External electrodes 6, 7 are formed on mutually opposite end faces on the outer surface of the ceramic laminate 5. Further, the external electrodes 6, 7 are respectively connected to the internal electrodes 3, 4 which are alternately led to the end faces on the opposite sides.

再者,作為構成外部電極6、7之導電材料,例如可使用以Ag或Cu為主成分者等。 Further, as the conductive material constituting the external electrodes 6 and 7, for example, Ag or Cu as a main component can be used.

再者,該實施形態1之積層陶瓷電容器1係具備2個外部電極6、7之二端子型者,但本發明亦可應用於具備多個外部電極之多端子型之構成者。 Further, the multilayer ceramic capacitor 1 of the first embodiment includes two terminal types of two external electrodes 6 and 7. However, the present invention can also be applied to a multi-terminal type having a plurality of external electrodes.

於該積層陶瓷電容器1中,內部電極3、4以Ni為主成分,且含有Sn。 In the multilayer ceramic capacitor 1, the internal electrodes 3 and 4 contain Ni as a main component and contain Sn.

而且,構成為內部電極3、4之自與陶瓷介電層2對向之表面起深度為20nm之區域(界面附近區域)內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上。 Further, the ratio of Sn in the region (the vicinity of the interface) from the surface facing the ceramic dielectric layer 2 to the surface of the internal electrodes 3 and 4 with respect to the sum of Sn and Ni is Sn/(Ni). The ratio of +Sn) to the region of 0.001 or more in terms of the molar ratio is 75% or more.

又,構成為內部電極3、4之厚度方向之中央區域(電極內部區域)內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%。 Further, the ratio of Sn in the central region (electrode inner region) in the thickness direction of the internal electrodes 3 and 4 to the total amount of Sn and Ni, that is, the Sn/(Ni+Sn) ratio is 0.001 or more in terms of the molar ratio. The proportion of the area is less than 40%.

藉由設為此種構成,可獲得如下積層陶瓷電容器1:能夠獲得高靜電電容,且高溫負荷壽命優異、可靠性高。 With such a configuration, the laminated ceramic capacitor 1 can be obtained in which a high electrostatic capacitance can be obtained, and the high-temperature load life is excellent and the reliability is high.

<積層陶瓷電容器之製造> <Manufacture of laminated ceramic capacitors>

其次,對上述本發明之一實施形態(實施形態1)之積層陶瓷電容器1之製造方法進行說明。 Next, a method of manufacturing the multilayer ceramic capacitor 1 according to the embodiment (the first embodiment) of the present invention will be described.

(1)首先,稱量特定量之BaCO3粉末與TiO2粉末作為含有Ti與Ba之鈣鈦礦(perovskite)型化合物之原料。接著將所稱量之粉末調和,並藉由球磨機混合後,於特定之條件下進行熱處理,藉此獲得成為構成陶瓷介電層之材料之主成分之鈦酸鋇系鈣鈦礦型化合物粉末。 (1) First, a specific amount of BaCO 3 powder and TiO 2 powder are weighed as a raw material of a perovskite type compound containing Ti and Ba. Then, the weighed powder is blended, and after being mixed by a ball mill, heat treatment is performed under specific conditions to obtain a barium titanate-based perovskite-type compound powder which is a main component of a material constituting the ceramic dielectric layer.

(2)其次,準備作為副成分之Dy2O3、MgO、MnO、SiO2之各粉末,並以相對於上述主成分100莫耳份,Dy2O3為0.75莫耳份,MgO為1莫耳份,MnO為0.2莫耳份,SiO2為1莫耳份之方式進行稱量。將該等粉末與主成分之鈦酸鋇系鈣鈦礦型化合物粉末進行調配,且利用球磨機混合一定時間並乾燥後,進行乾式粉碎,從而獲得原料粉末。 (2) Next, each powder of Dy 2 O 3 , MgO, MnO, and SiO 2 as an auxiliary component is prepared, and Dy 2 O 3 is 0.75 mol parts and MgO is 1 with respect to 100 parts of the main component. The molar fraction was measured in such a manner that MnO was 0.2 mol parts and SiO 2 was 1 mol. These powders are blended with a barium titanate-based perovskite-type compound powder of a main component, and after being mixed by a ball mill for a predetermined period of time and dried, dry-pulverization is carried out to obtain a raw material powder.

(3)其次,於該原料粉末中添加聚乙烯醇縮丁醛系黏合劑及乙醇等有機溶劑,並利用球磨機進行濕式混合,調整漿料。藉由刮刀法(doctor blade method)將該陶瓷漿料成形為片材,而獲得厚度為2.8μm之陶瓷生片。 (3) Next, a polyvinyl butyral based binder and an organic solvent such as ethanol are added to the raw material powder, and the mixture is wet-mixed by a ball mill to adjust the slurry. The ceramic slurry was formed into a sheet by a doctor blade method to obtain a ceramic green sheet having a thickness of 2.8 μm.

(4)其次,利用以下方法製備內部電極形成用之導電膏。 (4) Next, a conductive paste for forming an internal electrode was prepared by the following method.

首先,製備用以調配於內部電極形成用之導電膏之相同材料(Sn成分調配相同材料)。於製備該Sn成分調配相同材料時,準備表面積為35m2/g之鈦酸鋇(BaTiO3)粉末與SnO2粉末,以Sn相對於鈦酸鋇(BaTiO3)之量成為如表1所示之比例之方式進行調製,並利用球磨機進行濕式混合後,進行粉碎。繼而,於將所獲得之漿料蒸發乾燥後,進行乾式粉碎,從而獲得用以調配於內部電極形成用之導電膏之Sn成分調配相同材料。 First, the same material (Sn composition is blended with the same material) for the conductive paste for internal electrode formation is prepared. When preparing the Sn component to prepare the same material, a barium titanate (BaTiO 3 ) powder having a surface area of 35 m 2 /g and a SnO 2 powder were prepared, and the amount of Sn relative to barium titanate (BaTiO 3 ) was as shown in Table 1. The ratio is adjusted in such a manner that it is wet-mixed by a ball mill and then pulverized. Then, after the obtained slurry was evaporated and dried, dry pulverization was carried out to obtain a Sn material which was prepared for the conductive paste for forming an internal electrode, and the same material was blended.

再者,表1之所謂「相同材料中之Sn相對於鈦酸鋇之比例」係表示相同材料中之Sn之量(莫耳量(mol量))相對於BaTiO3之量(莫耳量)之比例之值,且係藉由下述式:Sn之比例={Sn(莫耳量)/BaTiO3(莫耳量)}×100 Further, the phrase "the ratio of Sn to barium titanate in the same material" in Table 1 means the amount of Sn (molar amount (mol amount)) in the same material relative to the amount of BaTiO 3 (molar amount). The ratio of the ratio is determined by the following formula: the ratio of Sn = {Sn (mole) / BaTiO 3 (mole)} × 100

而求出之值。 And find the value.

又,作為導電性粉末,準備Ni粉末與Ni-Sn合金粉末(Ni:Sn=99:1)。 Further, as the conductive powder, Ni powder and Ni-Sn alloy powder (Ni:Sn=99:1) were prepared.

繼而,以上述Sn成分調配相同材料相對於Ni粉末之重量比、或相對於Ni-Sn合金粉末之重量比成為如表1所示之重量比之方式,稱量Sn成分調配相同材料、Ni粉末、及Ni-Sn合金粉末。 Then, the weight ratio of the same material to the Ni powder or the weight ratio of the Ni-Sn alloy powder to the Sn composition is set to a weight ratio as shown in Table 1, and the Sn component is weighed to prepare the same material, Ni powder. And Ni-Sn alloy powder.

接著,添加聚乙烯醇縮丁醛系黏合劑及乙醇等有機溶劑,並利用球磨機進行濕式混合,藉此獲得內部電極形成用之導電膏。 Next, a polyvinyl butyral based adhesive and an organic solvent such as ethanol are added and wet-mixed by a ball mill to obtain a conductive paste for forming an internal electrode.

再者,表1之所謂「相同材料相對於Ni之比例」係表示內部電極形成用之導電膏中之相同材料之重量份相對於Ni100重量份之比例之值,且係藉由下述式:相同材料相對於Ni之比例={相同材料(重量份)/Ni重量份}×100 In addition, the "ratio of the same material to Ni" in Table 1 means the value of the ratio of the weight part of the same material in the electrically conductive paste for internal electrode formation to 100 parts by weight of Ni, and is represented by the following formula: The ratio of the same material to Ni = {same material (parts by weight) / Ni parts by weight} × 100

而求出之值。 And find the value.

(5)其次,將該導電膏以特定之圖案印刷於以上述方式製作之陶瓷生片上,從而形成煅燒後成為內部電極之導電膏層(內部電極圖案)。 (5) Next, the conductive paste is printed on the ceramic green sheet produced in the above manner in a specific pattern to form a conductive paste layer (internal electrode pattern) which becomes an internal electrode after firing.

(6)接著,將陶瓷生片以上述內部電極圖案之被引出之側交替地成為相反側之方式積層複數片,從而獲得未煅燒之陶瓷積層體。 (6) Next, the ceramic green sheets are laminated in a plurality of sheets so that the side on which the internal electrode patterns are drawn are alternately turned to the opposite side, thereby obtaining an unfired ceramic laminate.

(7)將該陶瓷積層體於N2氣氛中加熱至350℃,使黏合劑燃燒後,於氧分壓為10-10~10-12MPa之含有H2-N2-H2O氣體之還原氣氛中以20℃/min之升溫速度使其升溫,並於1200℃下煅燒20分鐘,藉此獲得煅燒過之陶瓷積層體。 (7) heating the ceramic laminate to a temperature of 350 ° C in a N 2 atmosphere to burn the binder, and then containing H 2 -N 2 -H 2 O gas at a partial pressure of oxygen of 10 -10 to 10 -12 MPa. The temperature was raised in a reducing atmosphere at a temperature elevation rate of 20 ° C/min, and calcined at 1200 ° C for 20 minutes, thereby obtaining a calcined ceramic laminate.

(8)其次,於所獲得之陶瓷積層體之兩端面塗佈以Ag作為導電成分、且含有B2O3-SiO2-BaO系玻璃料之外部電極形成用之導電膏,且於N2氣氛中以600℃之溫度進行燒接,藉此形成與內部電極電性連接之外部電極。藉此獲得具有如圖1所示之構造之積層陶瓷電容器(表1之試樣編號1~9之試樣)1。 (8) Next, a conductive paste for forming an external electrode containing Ag as a conductive component and containing a B 2 O 3 -SiO 2 -BaO-based glass frit is coated on both end faces of the obtained ceramic laminate, and is N 2 The atmosphere is baked at a temperature of 600 ° C to form an external electrode electrically connected to the internal electrode. Thus, a multilayer ceramic capacitor having the structure shown in Fig. 1 (sample Nos. 1 to 9 of Table 1) 1 was obtained.

再者,表1之對試樣編號標註有*之試樣編號4~9之試樣為不滿足本發明之要件之比較例之試樣,表1之未對試樣編號標註*之試樣編號1~3之試樣為滿足本發明之要件之實施例之試樣。 Further, the samples of the sample Nos. 4 to 9 in which the sample numbers are marked with * in Table 1 are samples which do not satisfy the requirements of the present invention, and the samples of Table 1 which are not marked with the sample number * The samples Nos. 1 to 3 are samples satisfying the examples of the requirements of the present invention.

再者,於該實施形態1中獲得之積層陶瓷電容器之外形尺寸為寬度(W):1.2mm、長度(L):2.0mm、厚度(T):1.1mm,介存於內部電極間之陶瓷介電層之厚度為2.2μm。又,介存於內部電極間之有效陶瓷介電層之總數為300層,每一層之對向電極之面積為1.6×10-6m2Further, the multilayer ceramic capacitor obtained in the first embodiment has a width (W) of 1.2 mm, a length (L) of 2.0 mm, and a thickness (T) of 1.1 mm, which are interposed between the internal electrodes. The thickness of the dielectric layer was 2.2 μm. Further, the total number of effective ceramic dielectric layers interposed between the internal electrodes was 300, and the area of the counter electrode of each layer was 1.6 × 10 -6 m 2 .

<特性之評價> <Evaluation of characteristics>

利用以下說明之方法,對以上述方式製作之各積層陶瓷電容器(表1之試樣編號1~9之試樣)進行靜電電容之測定或高溫負荷試驗等,並調查特性。 Each of the laminated ceramic capacitors produced in the above-described manner (samples of sample Nos. 1 to 9 in Table 1) was subjected to measurement of electrostatic capacitance or high-temperature load test by the method described below, and the characteristics were investigated.

(1)靜電電容之測定 (1) Determination of electrostatic capacitance

首先,自所製作之表1之試樣編號1~9之試樣(積層陶瓷電容器)中分別取樣10個試樣。 First, 10 samples were sampled from the sample Nos. 1 to 9 (layered ceramic capacitor) of Table 1 produced.

其次,使用自動橋式測定器,於AC(A1ternating Current,交流)電壓1Vrms、1kHz之條件下測定靜電電容。 Next, the electrostatic capacitance was measured under the conditions of an AC (A1ternating Current) voltage of 1 Vrms and 1 kHz using an automatic bridge type measuring device.

將其結果一併示於表1。 The results are shown together in Table 1.

(2)高溫負荷試驗 (2) High temperature load test

對已測定過靜電電容之試樣,進而於165℃、7.5V之條件下進行高溫負荷試驗,將絕緣電阻達到10KΩ以下之時間判定為故障。根據該故障時間算出MTTF(Mean Time To Failure,平均無故障時間)。 The sample having the measured electrostatic capacitance was further subjected to a high-temperature load test at 165 ° C and 7.5 V, and the time when the insulation resistance was 10 KΩ or less was judged as a failure. The MTTF (Mean Time To Failure) is calculated based on the failure time.

將其結果一併示於表1。 The results are shown together in Table 1.

(3)內部電極中之Sn之存在及分佈狀態之確認 (3) Confirmation of the existence and distribution of Sn in the internal electrode

又,使用製造積層陶瓷電容器時之於上述(7)之步驟中所獲得的煅燒過之陶瓷積層體,利用以下說明之方法確認Sn存在於內部電極中 且與Ni合金化之情況、及內部電極中之Sn之分佈狀態。 Further, using the calcined ceramic laminate obtained in the above step (7) in the production of the multilayer ceramic capacitor, it was confirmed by the method described below that Sn exists in the internal electrode. The state of alloying with Ni and the distribution state of Sn in the internal electrode.

(3-1)內部電極中之Sn之確認 (3-1) Confirmation of Sn in the internal electrode

(a)研磨 (a) grinding

以如長度(L)方向沿著垂直方向之姿勢保持各試樣,且以樹脂加固試樣之周圍,使由試樣之寬度(W)與厚度(T)規定之WT面自樹脂露出。 Each sample was held in a vertical direction as in the length (L) direction, and the periphery of the sample was reinforced with a resin so that the WT surface defined by the width (W) and the thickness (T) of the sample was exposed from the resin.

接著,藉由研磨機對各試樣之WT面進行研磨,研磨至各試樣之長度(L)方向之1/2左右之深度為止。繼而,為了消除研磨所致之內部電極之毛邊,而於研磨結束後藉由離子研磨對研磨表面進行加工。 Next, the WT surface of each sample was polished by a grinder, and polished to a depth of about 1/2 of the length (L) direction of each sample. Then, in order to eliminate the burrs of the internal electrodes due to the grinding, the abrasive surface is processed by ion milling after the polishing is completed.

(b)內部電極之映射分析 (b) Mapping analysis of internal electrodes

接著,如圖2所示,於WT剖面之L方向1/2左右之位置上之積層有內部電極之區域中的中央區域9、及靠近上下之外層部(無效部)之區域即上部區域8及下部區域10之3個區域內,利用WDX(Wavelength Dispersive X-Ray Spectrometer,波長色散X射線光譜法)進行Ni及Sn之映射分析。 Next, as shown in FIG. 2, the central region 9 in the region where the internal electrodes are laminated in the L direction of the WT cross section, and the upper region 8 in the region close to the upper and lower outer layer portions (ineffective portions) In the three regions of the lower region 10, mapping analysis of Ni and Sn was performed by WDX (Wavelength Dispersive X-Ray Spectrometer).

將針對試樣編號1之試樣(滿足本發明之要件之實施例之試樣)進行之Ni之映射分析之結果示於圖3,將Sn之映射分析之結果示於圖4。 The results of the mapping analysis of Ni for the sample of sample No. 1 (the sample satisfying the embodiment of the present invention) are shown in Fig. 3, and the results of the mapping analysis of Sn are shown in Fig. 4.

由圖3、圖4可確認於使用調配有Sn成分調配相同材料之導電膏而形成內部電極之試樣編號1之試樣(本發明之實施形態1之積層陶瓷電容器)中,在內部電極中存在Sn。 3 and 4, it can be confirmed that the sample of sample No. 1 (the multilayer ceramic capacitor of the first embodiment of the present invention) in which the internal electrode is formed by using the conductive paste of the same material in the Sn composition is used in the internal electrode. There is Sn.

再者,於使用有將Ni-Sn合金粉末作為導電成分、及將Ni粉末作為導電成分且含有調配有Sn成分(SnO2)之相同材料之導電膏的其他試樣(試樣編號2~8)之試樣、以及使用有不含調配有Sn成分(SnO2)之相同材料之導電膏的試樣編號9之試樣中之任一者之情形時,映射分析之結果均為確認於內部電極中存在Sn。 Further, other samples using a conductive paste containing Ni-Sn alloy powder as a conductive component and Ni powder as a conductive component and containing the same material as Sn component (SnO 2 ) were used (sample Nos. 2 to 8) The sample analysis and the sample of sample No. 9 using a conductive paste containing the same material as the Sn component (SnO 2 ), the results of the mapping analysis are confirmed inside. Sn is present in the electrode.

(3-2)內部電極中之Sn之形態之確認 (3-2) Confirmation of the form of Sn in the internal electrode

將製造積層陶瓷電容器時之於上述(7)之步驟中獲得之煅燒過之陶瓷積層體粉碎,使其成為粉末狀,並利用XRD(X ray diffraction,X射線繞射法)分析所獲得之粉末。其結果,Ni之峰值位置偏移,根據該情況,可確認內部電極中之Sn係以Ni與Sn之合金之形態存在。 The calcined ceramic laminate obtained in the above step (7) is pulverized in the production of the laminated ceramic capacitor, and is powdered, and the obtained powder is analyzed by XRD (X ray diffraction). . As a result, the peak position of Ni was shifted. According to this, it was confirmed that the Sn in the internal electrode exists in the form of an alloy of Ni and Sn.

(3-3)內部電極中之Sn之分佈狀態之確認 (3-3) Confirmation of the distribution state of Sn in the internal electrode

藉由研磨將製造積層陶瓷電容器時之於上述(7)之步驟中獲得之煅燒過之陶瓷積層體薄片化而製作分析試樣。接著,利用TEM(Transmission Electron Microscopy,穿透式電子顯微鏡)觀察該分析試樣,並自分析試樣中隨機選擇4根內部電極。 An analysis sample was prepared by flaking a calcined ceramic laminate obtained by the above step (7) in the production of a multilayer ceramic capacitor by polishing. Next, the analysis sample was observed by a TEM (Transmission Electron Microscopy), and four internal electrodes were randomly selected from the analysis sample.

繼而,自各內部電極之自與陶瓷介電層對向之表面起深度為20nm之區域(以下,稱為「界面附近區域」)、及內部電極之厚度方向上之中央區域(以下,稱為「電極內部區域」)之各者隨機抽選5個部位。 Then, a region having a depth of 20 nm from the surface facing the ceramic dielectric layer (hereinafter referred to as "the region near the interface") and a central region in the thickness direction of the internal electrode (hereinafter referred to as " Each of the electrode internal regions") was randomly selected from five locations.

其次,關於上述隨機選擇之4根內部電極,藉由EDX(Energy Dispersive X-ray Spectrometer,能量色散型X射線光譜法)對其界面附近區域與電極內部區域之各者之5個部位進行Ni與Sn之定量分析。各試樣之關於界面附近區域與電極內部區域之各者之資料數為4(內部電極之根數:4根)×5(界面附近區域與電極內部區域之各者之部位:5個部位)=20。 Next, regarding the four internal electrodes selected at random, the EDS (Energy Dispersive X-ray Spectrometer) is used to carry out Ni and the five parts of the vicinity of the interface and the internal region of the electrode. Quantitative analysis of Sn. The number of data of each sample in the vicinity of the interface and the inner region of the electrode was 4 (number of internal electrodes: 4) × 5 (part of the vicinity of the interface and the inner region of the electrode: 5 parts) =20.

根據分析結果之平均值求出Sn相對於Sn與Ni之合計量之比:Sn/(Ni+Sn)比(莫耳比)。 The ratio of Sn to the total amount of Sn and Ni was determined from the average of the analysis results: Sn/(Ni+Sn) ratio (Mohr ratio).

繼而,求出內部電極之界面附近區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例、及電極內部區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例。 Then, the ratio of Sn/(Ni+Sn) in the vicinity of the interface of the internal electrode to the region of 0.001 or more in terms of the molar ratio, and the ratio of Sn/(Ni+Sn) in the internal region of the electrode are determined as Mohr. The ratio is calculated as the ratio of the area of 0.001 or more.

將關於各試樣之內部電極之界面附近區域與電極內部區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例一併示於表1。 Table 1 shows the ratio of the Sn/(Ni+Sn) ratio in the vicinity of the interface of the internal electrode of each sample to the area in the electrode internal region of 0.001 or more in terms of the molar ratio.

如表1所示,於滿足界面附近區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上、且電極內部區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%這一本發明之要件的試樣編號1~3之試樣之情形時,經確認所獲得之靜電電容較大,可實現小型、高靜電電容,且高溫負荷試驗中之MTTF(平均無故障時間)之值較大,對於高溫下之使用之耐久性優異。 As shown in Table 1, the ratio of the Sn/(Ni+Sn) ratio in the vicinity of the interface to the region of 0.001 or more in terms of the molar ratio is 75% or more, and Sn/(Ni+Sn in the internal region of the electrode) When the ratio of the region of 0.001 or more in terms of the molar ratio is less than 40%, the sample of samples Nos. 1 to 3 of the requirements of the present invention is confirmed to have a large electrostatic capacitance, which can be realized. Small, high electrostatic capacitance, and the MTTF (mean time between failures) in the high temperature load test is large, and it is excellent in durability for use at high temperatures.

另一方面,於不滿足界面附近區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上、且電極內部區域內之Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%這一本發明之要件的試樣編號4~9之試樣之情形時,經確認於所取得之靜電電容或高溫負荷試驗中之耐久性之任一方面,結果均不理想。 On the other hand, the ratio of Sn/(Ni+Sn) in the region in the vicinity of the interface to the region of 0.001 or more in terms of the molar ratio is 75% or more, and Sn/(Ni+Sn) in the inner region of the electrode. In the case of samples of sample numbers 4 to 9 which are less than 40% of the area in which the molar ratio is 0.001 or more, which is confirmed in the obtained electrostatic capacitance or high temperature load test, In any aspect of durability, the results are not satisfactory.

再者,於使用有將Ni-Sn合金粉末作為導電成分、另一方面不含調配有Sn成分(SnO2)之相同材料之導電膏的試樣編號9之試樣之情形時,經確認關於高溫負荷試驗中之耐久性,雖可獲得良好之結果,但與滿足本發明之要件之試樣編號1~3之試樣之情形相比,所獲得之靜 電電容變小。 In addition, in the case of using the sample of sample No. 9 which has a Ni-Sn alloy powder as a conductive component and a conductive paste of the same material in which a Sn component (SnO 2 ) is blended on the other hand, it is confirmed that Although the durability in the high-temperature load test was good, the obtained electrostatic capacitance was smaller than that in the case of the samples Nos. 1 to 3 satisfying the requirements of the present invention.

由上述結果可知,根據本發明,可獲得如下積層陶瓷電容器:所獲得之靜電電容較大,並且高溫負荷試驗中之MTTF之值較大,耐久性優異。 From the above results, according to the present invention, it is possible to obtain a laminated ceramic capacitor in which the obtained electrostatic capacitance is large, and the value of MTTF in the high-temperature load test is large, and the durability is excellent.

再者,認為於本發明之積層陶瓷電容器中所獲得之靜電電容變大之原因在於:內部電極之界面附近區域內之Sn存在機率較電極內部區域高,於界面附近區域內,晶格中之晶格常數產生差,從而積層陶瓷電容器內部之殘留應力之分佈狀態產生變化。 Further, it is considered that the electrostatic capacitance obtained in the multilayer ceramic capacitor of the present invention is increased in that the existence probability of Sn in the vicinity of the interface of the internal electrode is higher than that in the internal region of the electrode, and in the vicinity of the interface, in the crystal lattice The lattice constant is poor, so that the distribution state of the residual stress inside the laminated ceramic capacitor changes.

又,認為於本發明之積層陶瓷電容器中高溫負荷試驗中之耐久性提高之原因在於:藉由內部電極之Ni-Sn合金化而使陶瓷介電層與內部電極之界面之狀態產生變化。推測尤其是於內部電極之與陶瓷介電層之界面存在Ni-Sn合金時對高溫負荷壽命之提高發揮重要作用。 Further, it is considered that the durability in the high-temperature load test of the multilayer ceramic capacitor of the present invention is improved in that the state of the interface between the ceramic dielectric layer and the internal electrode is changed by Ni-Sn alloying of the internal electrode. It is presumed that the presence of a Ni-Sn alloy at the interface between the internal electrode and the ceramic dielectric layer plays an important role in improving the high-temperature load life.

[實施形態2] [Embodiment 2]

於該實施形態2中,亦製造具有如圖1所示之構造之具備與本發明之實施形態1之積層陶瓷電容器相同之構成的積層陶瓷電容器。 In the second embodiment, a multilayer ceramic capacitor having the same configuration as that of the multilayer ceramic capacitor of the first embodiment of the present invention having the structure shown in Fig. 1 is also manufactured.

<積層陶瓷電容器之製造> <Manufacture of laminated ceramic capacitors>

其次,對本發明之實施形態2之積層陶瓷電容器1之製造方法進行說明。 Next, a method of manufacturing the multilayer ceramic capacitor 1 according to the second embodiment of the present invention will be described.

(1)首先,稱量特定量之BaCO3粉末與TiO2粉末作為含有Ti與Ba之鈣鈦礦型化合物之原料。接著將所稱量之粉末調和,並藉由球磨機混合一定時間後,於特定之條件下進行熱處理,藉此獲得成為構成陶瓷介電層之材料之主成分之鈦酸鋇系鈣鈦礦型化合物粉末。 (1) First, a specific amount of BaCO 3 powder and TiO 2 powder are weighed as a raw material of a perovskite-type compound containing Ti and Ba. Then, the weighed powder is blended, and after being mixed by a ball mill for a certain period of time, heat treatment is performed under specific conditions, thereby obtaining a barium titanate-based perovskite compound which is a main component of a material constituting the ceramic dielectric layer. powder.

(2)其次,準備作為副成分之Dy2O3、MgO、MnO、SiO2之各粉末,以相對於上述主成分100莫耳份,Dy2O3為0.75莫耳份,MgO為1莫耳份,MnO為0.2莫耳份,SiO2為1莫耳份之方式進行稱量。將該等粉末與主成分之鈦酸鋇系鈣鈦礦型化合物粉末進行調配,利用球磨機 混合一定時間並乾燥後,進行乾式粉碎,從而獲得原料粉末。 (2) Next, each powder of Dy 2 O 3 , MgO, MnO, and SiO 2 as an auxiliary component is prepared so as to be 100 parts by mole with respect to the above-mentioned main component 100, Dy 2 O 3 is 0.75 moles, and MgO is 1 mole. parts of the ear, MnO to 0.2 mole parts, SiO 2 were weighed to 1 molar parts of the embodiment. These powders are blended with the main component barium titanate-based perovskite-type compound powder, and mixed by a ball mill for a predetermined period of time and dried, followed by dry pulverization to obtain a raw material powder.

(3)其次,於該原料粉末中添加聚乙烯醇縮丁醛系黏合劑及乙醇等有機溶劑,並利用球磨機進行濕式混合,調整漿料。藉由刮刀法將該陶瓷漿料成形為片材,而獲得厚度為2.8μm之陶瓷生片。 (3) Next, a polyvinyl butyral based binder and an organic solvent such as ethanol are added to the raw material powder, and the mixture is wet-mixed by a ball mill to adjust the slurry. The ceramic slurry was formed into a sheet by a doctor blade method to obtain a ceramic green sheet having a thickness of 2.8 μm.

(4)其次,利用以下之方法製備內部電極形成用之導電膏。 (4) Next, a conductive paste for forming an internal electrode was prepared by the following method.

首先,製備用以調配於內部電極形成用之導電膏之相同材料(Sn成分調配相同材料)。於製備該Sn成分調配相同材料時,準備表面積為35m2/g之鈦酸鋇(BaTiO3)粉末與SnO2粉末,以Sn相對於鈦酸鋇(BaTiO3)之量成為如表2所示之比例之方式調製兩者,並利用球磨機進行濕式混合後,進行粉碎。繼而,於將所獲得之漿料蒸發乾燥後,進行乾式粉碎,從而獲得用以調配於內部電極形成用之導電膏之Sn成分調配相同材料。 First, the same material (Sn composition is blended with the same material) for the conductive paste for internal electrode formation is prepared. When preparing the Sn component to prepare the same material, a barium titanate (BaTiO 3 ) powder and a SnO 2 powder having a surface area of 35 m 2 /g were prepared, and the amount of Sn relative to barium titanate (BaTiO 3 ) was as shown in Table 2. The ratio was adjusted in such a manner that it was wet-mixed by a ball mill and then pulverized. Then, after the obtained slurry was evaporated and dried, dry pulverization was carried out to obtain a Sn material which was prepared for the conductive paste for forming an internal electrode, and the same material was blended.

再者,表2之所謂「相同材料中之Sn相對於BaTiO3之比例」係表示相同材料中之Sn之量(莫耳量)相對於BaTiO3之量(莫耳量)之比例之值,且係藉由下述式:Sn之比例={Sn(莫耳量)/BaTiO3(莫耳量)}×100 Further, the phrase "the ratio of Sn to BaTiO 3 in the same material" in Table 2 means the ratio of the amount of Sn (molar amount) to the amount of BaTiO 3 (molar amount) in the same material, And by the following formula: the ratio of Sn = {Sn (mole amount) / BaTiO 3 (mole amount) × 100

而求出之值。 And find the value.

又,準備Ni粉末作為導電性粉末,以Sn成分調配相同材料(亦簡稱為「相同材料」)相對於Ni粉末與上述Sn成分調配相同材料之合計量之比例成為如表2所示之比例之方式,稱量Sn成分調配相同材料及Ni粉末。 Further, Ni powder was prepared as a conductive powder, and the ratio of the total amount of the same material (also referred to as "the same material") to the Sn powder and the Sn material was adjusted to the ratio shown in Table 2 with the Sn component. In the manner, the Sn component was weighed to prepare the same material and Ni powder.

接著,添加聚乙烯醇縮丁醛系黏合劑及乙醇等有機溶劑,並利用球磨機進行濕式混合,藉此獲得內部電極形成用之導電膏。 Next, a polyvinyl butyral based adhesive and an organic solvent such as ethanol are added and wet-mixed by a ball mill to obtain a conductive paste for forming an internal electrode.

再者,表2之所謂「相同材料相對於Ni之比例」係表示內部電極形成用之導電膏中之Sn成分調配相同材料之重量份相對於Ni100重量份之比例之值,且係藉由下述式: 相同材料相對於Ni之比例={相同材料(重量份)/Ni重量份}×100 In addition, the "ratio of the same material to Ni" in Table 2 means the ratio of the weight ratio of the Sn component in the conductive paste for forming an internal electrode to the ratio of 100 parts by weight of Ni, and is Description: The ratio of the same material to Ni = {same material (parts by weight) / Ni parts by weight} × 100

而求出之值。 And find the value.

(5)其次,將該導電膏以特定之圖案印刷於以上述方式製作之陶瓷生片上,從而形成煅燒後成為內部電極之導電膏層(內部電極圖案)。 (5) Next, the conductive paste is printed on the ceramic green sheet produced in the above manner in a specific pattern to form a conductive paste layer (internal electrode pattern) which becomes an internal electrode after firing.

(6)接著,將陶瓷生片以上述內部電極圖案之被引出側交替地成為相反側之方式積層複數片,從而獲得未煅燒之陶瓷積層體。 (6) Next, the ceramic green sheets are laminated in a plurality of sheets so that the lead-out sides of the internal electrode patterns alternately become opposite sides, thereby obtaining an unfired ceramic laminate.

(7)將該陶瓷積層體於N2氣氛中加熱至350℃,使黏合劑燃燒後,於氧分壓為10-10~10-12MPa之含有H2-N2-H2O氣體之還原氣氛中以20℃/min之升溫速度使其升溫,且於1200℃下煅燒20分鐘,藉此獲得煅燒過之陶瓷積層體。 (7) heating the ceramic laminate to a temperature of 350 ° C in a N 2 atmosphere to burn the binder, and then containing H 2 -N 2 -H 2 O gas at a partial pressure of oxygen of 10 -10 to 10 -12 MPa. The temperature was raised at a temperature elevation rate of 20 ° C / min in a reducing atmosphere, and calcined at 1200 ° C for 20 minutes, thereby obtaining a calcined ceramic laminate.

(8)其次,於所獲得之陶瓷積層體之兩端面塗佈以Ag作為導電成分且含有B2O3-SiO2-BaO系玻璃料之外部電極形成用之導電膏,且於N2氣氛中以600℃之溫度進行燒接,藉此形成與內部電極電性連接之外部電極。藉此,獲得具有如圖1所示之構造之積層陶瓷電容器(表2之試樣編號11~19之試樣)。其中,試樣編號19之試樣係使用以Ni-Sn合金粉末作為導電成分之內部電極形成用之導電膏而形成內部電極。 (8) Next, a conductive paste for forming an external electrode containing B 2 O 3 -SiO 2 -BaO-based glass frit, which is made of Ag as a conductive component and having Ag as a conductive component, is applied to both end faces of the obtained ceramic laminate, and is in a N 2 atmosphere. The middle portion is fired at a temperature of 600 ° C to form an external electrode electrically connected to the internal electrode. Thereby, a multilayer ceramic capacitor having the structure shown in Fig. 1 (samples of sample Nos. 11 to 19 of Table 2) was obtained. In the sample No. 19, a conductive paste for forming an internal electrode using a Ni—Sn alloy powder as a conductive component was used to form an internal electrode.

再者,表2之對試樣編號標註有*之試樣編號14~19之試樣為不滿足本發明之要件之比較例之試樣,表2之未對試樣編號標註*之試樣編號11~13之試樣為滿足本發明之要件之實施例之試樣。 Further, the sample of the sample No. 14 to 19 in which the sample number is marked with * in Table 2 is a sample of a comparative example which does not satisfy the requirements of the present invention, and the sample of the table 2 which is not marked with the number of the sample * The samples Nos. 11 to 13 are samples satisfying the examples of the requirements of the present invention.

再者,於該實施形態2中獲得之積層陶瓷電容器之外形尺寸係與實施形態1之情形相同,為寬度(W):1.2mm、長度(L)=2.0mm、厚度(T):1.1mm,介存於內部電極間之陶瓷介電層之厚度為2.2μm,又,介存於內部電極間之有效陶瓷介電層之總數為300層,每一層之對向電極之面積為1.6×10-6m2In addition, the dimensions of the multilayer ceramic capacitor obtained in the second embodiment are the same as those in the first embodiment, and are width (W): 1.2 mm, length (L) = 2.0 mm, and thickness (T): 1.1 mm. The thickness of the ceramic dielectric layer interposed between the internal electrodes is 2.2 μm, and the total number of effective ceramic dielectric layers interposed between the internal electrodes is 300, and the area of the counter electrode of each layer is 1.6×10. -6 m 2 .

<特性之評價> <Evaluation of characteristics>

利用以下說明之方法對以上述方式製作之各積層陶瓷電容器(表2之試樣編號11~19之試樣)進行靜電電容之測定或高溫負荷試驗等,並調查特性。 Each of the laminated ceramic capacitors produced in the above-described manner (samples of sample Nos. 11 to 19 in Table 2) was subjected to measurement of electrostatic capacitance or high-temperature load test by the method described below, and the characteristics were investigated.

(1)靜電電容之測定 (1) Determination of electrostatic capacitance

首先,自所製作之表2之試樣編號11~19之試樣(積層陶瓷電容器)中分別取樣10個試樣。 First, 10 samples were sampled from the samples (layered ceramic capacitors) of the sample Nos. 11 to 19 of Table 2 produced.

其次,使用自動橋式測定器,於AC電壓1Vrms、1kHz之條件下測定靜電電容。 Next, the electrostatic capacitance was measured under the conditions of an AC voltage of 1 Vrms and 1 kHz using an automatic bridge type measuring device.

將其結果一併示於表2。 The results are shown together in Table 2.

(2)高溫負荷試驗 (2) High temperature load test

對已測定過靜電電容之試樣,進而於165℃、7.5V之條件下進行高溫負荷試驗,將絕緣電阻達到10KΩ以下之時間判定為故障。根據該故障時間算出MTTF(平均無故障時間)。 The sample having the measured electrostatic capacitance was further subjected to a high-temperature load test at 165 ° C and 7.5 V, and the time when the insulation resistance was 10 KΩ or less was judged as a failure. The MTTF (mean time between failures) is calculated based on the failure time.

將其結果一併示於表2。 The results are shown together in Table 2.

(3)內部電極中之Sn之存在及分佈狀態之確認 (3) Confirmation of the existence and distribution of Sn in the internal electrode

又,使用製造積層陶瓷電容器時之於上述(7)之步驟中所獲得之 煅燒過之陶瓷積層體,藉由以下說明之方法確認Sn存在於內部電極中且與Ni合金化之情況、及內部電極中之Sn之分佈狀態。 Further, when the multilayer ceramic capacitor is manufactured, the step obtained in the above step (7) is used. The calcined ceramic laminate was confirmed by the method described below in the case where Sn was present in the internal electrode and alloyed with Ni, and the distribution state of Sn in the internal electrode.

(3-1)內部電極中之Sn之確認 (3-1) Confirmation of Sn in the internal electrode

(a)研磨 (a) grinding

以如長度(L)方向沿著垂直方向之姿勢保持各試樣,且以樹脂加固試樣之周圍,使由試樣之寬度(W)與厚度(T)規定之WT面自樹脂露出。 Each sample was held in a vertical direction as in the length (L) direction, and the periphery of the sample was reinforced with a resin so that the WT surface defined by the width (W) and the thickness (T) of the sample was exposed from the resin.

接著,利用研磨機對各試樣之WT面進行研磨,研磨至各試樣之長度(L)方向之1/2左右之深度為止。繼而,為了消除研磨所致之內部電極之毛邊,而於研磨結束後藉由離子研磨對研磨表面進行加工。 Next, the WT surface of each sample was polished by a grinder and polished to a depth of about 1/2 of the length (L) direction of each sample. Then, in order to eliminate the burrs of the internal electrodes due to the grinding, the abrasive surface is processed by ion milling after the polishing is completed.

(b)內部電極之映射分析 (b) Mapping analysis of internal electrodes

接著,與實施形態1之情形同樣地,如圖2所示,於WT剖面之L方向1/2左右之位置上之積層有內部電極之區域中的中央區域9、及靠近上下之外層部(無效部)之區域即上部區域8及下部區域10之3個區域內,藉由WDX(波長色散X射線光譜法)進行Ni及Sn之映射分析。 Next, as in the case of the first embodiment, as shown in FIG. 2, the central region 9 in the region where the internal electrodes are laminated at the position of about 1/2 of the L direction of the WT section, and the upper and lower layers are adjacent to each other ( In the region of the ineffective portion, that is, in the three regions of the upper region 8 and the lower region 10, mapping analysis of Ni and Sn is performed by WDX (wavelength dispersive X-ray spectroscopy).

上述映射分析之結果為,於使用調配有Sn成分調配相同材料之導電膏而形成內部電極之具備本發明之要件之試樣編號11~13之試樣中,經確認於內部電極中存在Sn。 As a result of the above-described mapping analysis, it was confirmed that Sn was present in the internal electrode in the samples No. 11 to 13 having the requirements of the present invention in which the conductive paste of the same material was blended to form the internal electrode.

再者,於不具備本發明之要件之試樣編號14~18之試樣、及使用有不含調配有Sn成分(SnO2)之相同材料之導電膏之試樣編號19之試樣中之任一者之情形時,映射分析之結果均為確認於內部電極中存在Sn。 Further, in the sample Nos. 14 to 18 which do not have the requirements of the present invention, and the sample No. 19 in which the conductive paste containing the same material as the Sn component (SnO 2 ) is not contained, In either case, the result of the mapping analysis confirmed that Sn was present in the internal electrode.

(3-2)內部電極中之Sn之形態之確認 (3-2) Confirmation of the form of Sn in the internal electrode

將製造積層陶瓷電容器時之於上述(7)之步驟中所獲得之煅燒過之陶瓷積層體粉碎,使其成為粉末狀,並藉由XRD(X射線繞射法)分析所獲得之粉末。其結果,Ni之峰值位置偏移,根據該情況,可確認 內部電極中之Sn係以Ni與Sn之合金之形態存在。 The calcined ceramic laminate obtained in the above step (7) when the multilayer ceramic capacitor was produced was pulverized to be powdery, and the obtained powder was analyzed by XRD (X-ray diffraction method). As a result, the peak position of Ni is shifted, and based on this, it can be confirmed. The Sn in the internal electrode exists in the form of an alloy of Ni and Sn.

(3-3)內部電極中之Sn之分佈狀態之確認 (3-3) Confirmation of the distribution state of Sn in the internal electrode

如圖2所示,對於WT剖面之L方向1/2左右之位置上之積層有內部電極之區域中的中央區域9、及靠近上下之外層部(無效部)之區域即上部區域8及下部區域10之3個區域之各者,使用利用FIB(Focused Ion Beam,聚焦離子束)之微取樣加工法準備經薄片化之分析試樣。 As shown in Fig. 2, the central region 9 in the region where the internal electrodes are laminated in the L direction of the WT cross section, and the upper region 8 and the lower portion in the region close to the upper and lower outer layer portions (ineffective portions) Each of the three regions of the region 10 was prepared using a FIB (Focused Ion Beam) microsampling process to prepare a sliced analysis sample.

經薄片化之試樣係以其厚度成為60nm以下之方式加工而成。再者,FIB加工時所形成之試樣表面之變質層係藉由Ar離子研磨而去除。 The thinned sample was processed to have a thickness of 60 nm or less. Furthermore, the altered layer on the surface of the sample formed during FIB processing is removed by Ar ion milling.

於FIB下降時,使用SMI3050SE(Seiko Instruments公司製造),於Ar離子研磨時,使用PIPS(Gatan公司製造)。 When the FIB was lowered, SMI3050SE (manufactured by Seiko Instruments Co., Ltd.) was used, and at the time of Ar ion polishing, PIPS (manufactured by Gatan Co., Ltd.) was used.

利用STEM(Scanning Transmission Electron Microscopy,掃描穿透式電子顯微鏡)觀察以上述方式製作之試樣(薄片化試樣),且自針對各區域之各者而準備之試樣中選擇4根不同之內部電極。繼而,於相對於薄片化試樣之剖面大致垂直之陶瓷元件與內部電極之界面尋找5個部位。 The sample (sheet-formed sample) prepared as described above was observed by STEM (Scanning Transmission Electron Microscopy), and four different internal parts were selected from samples prepared for each of the respective regions. electrode. Then, five locations were found at the interface between the ceramic element and the internal electrode which were substantially perpendicular to the cross section of the thinned sample.

繼而,將與該大致垂直之界面接觸之內部電極劃分成自該界面起向內部電極內部深入2nm之區域、及自該界面起向內部電極內部深入20nm以上之區域。 Then, the internal electrode that is in contact with the substantially perpendicular interface is divided into a region deeper than 2 nm from the interface toward the inside of the internal electrode, and a region deeper than 20 nm from the interface toward the inside of the internal electrode.

再者,上述相對於薄片化試樣之剖面大致垂直之界面係以如下方式尋找。藉由STEM(掃描穿透式電子顯微鏡)觀察顯露於界面之兩側之線、即菲涅耳條紋(Fresnel fringe),尋找使焦點變化時菲涅耳條紋之對比度於兩側大致對稱地變化之界面,並將其設為相對於薄片化試樣剖面大致垂直之界面。 Further, the above-mentioned interface which is substantially perpendicular to the cross section of the flaky sample is found in the following manner. The STEM (scanning transmission electron microscope) is used to observe the Fresnel fringe which is exposed on both sides of the interface, and finds that the contrast of the Fresnel fringes changes substantially symmetrically on both sides when the focus changes. The interface is set to be an interface that is substantially perpendicular to the cross-section of the exfoliated sample.

又,於STEM分析時,使用JEM-2200FS(JEOL製造)作為掃描穿透式電子顯微鏡。加速電壓為200kV。 Further, in the STEM analysis, JEM-2200FS (manufactured by JEOL) was used as a scanning transmission electron microscope. The acceleration voltage is 200kV.

檢測器係使用JED-2300T且60mm2口徑之SDD(Silicon Drift Detector,矽漂移檢測器)檢測器,EDX系統係使用Noran System7(Thermo Fisher Scientific公司製造)。 The detector was a JED-2300T and a 60 mm 2 gauge SDD (Silicon Drift Detector) detector, and the EDX system was a Noran System 7 (manufactured by Thermo Fisher Scientific).

繼而,對於自上述界面起向內部電極內部深入2nm之區域及自界面起向內部電極內部深入20nm之區域之各者,於5部位×4根之合計20個部位中,使用EDX(能量色散型X射線分析裝置)實施Ni與Sn之定量分析。電子束之測定探針直徑係設為約1nm,測定時間係設為30秒。再者,自所獲得之EDX光譜之定量修正係使用Cliff-Lorimer修正。 Then, EDX (Energy Dispersion Type) is used in a total of 20 locations of 5 locations × 4 in a region in which the internal electrode is deeper by 2 nm from the interface and a region deeper than 20 nm from the interface to the inside of the internal electrode. X-ray analysis apparatus) performs quantitative analysis of Ni and Sn. The electron beam measurement probe diameter was set to about 1 nm, and the measurement time was set to 30 seconds. Furthermore, quantitative corrections from the obtained EDX spectra were corrected using Cliff-Lorimer.

於圖5中表示陶瓷介電層與內部電極之界面附近之Sn之STEM-EDX映像。再者,映射時間係設為3小時。 A STEM-EDX image of Sn near the interface between the ceramic dielectric layer and the internal electrodes is shown in FIG. Furthermore, the mapping time is set to 3 hours.

由圖5可知,於陶瓷介電層與內部電極之界面附近存在多於內部電極之內部之Sn。 As can be seen from Fig. 5, there is more Sn inside the internal electrode than the interface between the ceramic dielectric layer and the internal electrode.

再者,就於該實施形態2中製作之各試樣之耐久性而言,如表2所示,於滿足本發明之要件之試樣編號11~13之試樣(積層陶瓷電容器)之情形時,經確認MTTF之值較大,可靠性提高,認為其原因在於,藉由內部電極之Ni-Sn合金化使陶瓷與電極之界面之狀態產生變化。 In addition, as for the durability of each sample produced in the second embodiment, as shown in Table 2, in the case of the sample No. 11 to 13 satisfying the requirements of the present invention (the laminated ceramic capacitor) When the value of the MTTF was confirmed to be large and the reliability was improved, it was considered that the reason was that the state of the interface between the ceramic and the electrode was changed by Ni-Sn alloying of the internal electrode.

又,於滿足本發明之要件之試樣編號11~13之試樣(積層陶瓷電容器)之情形時,經確認可獲得大的靜電電容。認為其原因在於,於內部電極之自與陶瓷介電層之界面起深度為2nm之區域內,Sn以較自界面起深度為20nm以上之區域高1.0原子%以上之濃度存在,藉此使積層陶瓷電容器內部之殘留應力之分佈狀態產生變化。 Further, in the case of the sample (the multilayer ceramic capacitor) of the sample Nos. 11 to 13 which satisfies the requirements of the present invention, it was confirmed that a large electrostatic capacitance can be obtained. The reason is considered to be that in the region where the internal electrode is at a depth of 2 nm from the interface with the ceramic dielectric layer, Sn is present at a concentration of 1.0 atom% or more higher than the region having a depth of 20 nm or more from the interface, thereby allowing the layer to be laminated. The distribution state of the residual stress inside the ceramic capacitor changes.

另一方面,於在實施形態2中製作之不滿足本發明之要件之試樣(試樣編號14~19之試樣)之情形時,經確認於靜電電容及耐久性(MTTF)之至少一者結果欠佳。 On the other hand, in the case of the sample (sample Nos. 14 to 19) which is produced in the second embodiment and does not satisfy the requirements of the present invention, it is confirmed that at least one of the capacitance and the durability (MTTF) is confirmed. The result is not good.

再者,於本發明之積層陶瓷電容器中,亦可在陶瓷介電層與內部電極之界面存在Ni與Sn以外之陶瓷或內部電極所含有之元素。又,於陶瓷介電層與內部電極之界面之一部分亦可存在由Ni與Sn以外構成之異相。 Further, in the multilayer ceramic capacitor of the present invention, an element contained in a ceramic or an internal electrode other than Ni and Sn may be present at the interface between the ceramic dielectric layer and the internal electrode. Further, a part of the interface between the ceramic dielectric layer and the internal electrode may have a different phase other than Ni and Sn.

進而,內部電極用之相同材料既可與構成陶瓷介電層之陶瓷材料粉末為相同組成,亦可不含一部分之構成元素,或亦可一部分之構成元素不同,又,亦可調配比率不同。 Further, the same material for the internal electrode may have the same composition as the ceramic material powder constituting the ceramic dielectric layer, or may not contain a part of the constituent elements, or may be different from a part of the constituent elements, or may have different ratios.

又,構成陶瓷介電層之陶瓷材料及構成相同材料之陶瓷材料較理想為以鈣鈦礦型氧化物為主成分者。於上述實施形態中,使用作為鈣鈦礦型氧化物之BaTiO3作為陶瓷材料,但亦能夠以Ca或Sr取代構成BaTiO3之Ba之一部分,或以Zr取代構成BaTiO3之Ti之一部分。又,亦可使用CaZrO3等其他鈣鈦礦型化合物。 Further, the ceramic material constituting the ceramic dielectric layer and the ceramic material constituting the same material are preferably those having a perovskite-type oxide as a main component. In the above embodiment, BaTiO 3 which is a perovskite-type oxide is used as the ceramic material, but it is also possible to substitute one of Ba which constitutes BaTiO 3 with Ca or Sr or a part of Ti which constitutes BaTiO 3 with Zr. Further, other perovskite-type compounds such as CaZrO 3 may also be used.

又,自內部電極與陶瓷介電層之界面起向內部電極側深入2nm之區域內之Sn相對於Sn與Ni之合計量之比例超過2原子%,若更高則對高溫負荷壽命之提高而言較為理想,因而並無特別上限。其原因在於,認為Sn之比例越高,則陶瓷介電層與內部電極之界面之狀態(電性障壁高度)之變化程度越大。再者,於自上述界面起向內部電極側深入2nm之區域內之Sn之比例為例如20原子%以上之情形時亦可獲得效果。 Further, the ratio of Sn to the total amount of Sn and Ni in the region deeper than 2 nm from the interface between the internal electrode and the ceramic dielectric layer to the internal electrode side exceeds 2 atom%, and if it is higher, the high-temperature load life is improved. The statement is ideal and there is no special ceiling. The reason for this is that the higher the ratio of Sn, the greater the degree of change in the state of the interface between the ceramic dielectric layer and the internal electrode (electrical barrier height). In addition, when the ratio of Sn in the region deeper than 2 nm from the interface to the internal electrode side is, for example, 20 atom% or more, an effect can be obtained.

本發明進而於其他方面亦不限定於上述實施形態,關於構成陶瓷積層體之陶瓷介電層或內部電極之層數等,可於發明之範圍內添加各種應用、變形。 The present invention is not limited to the above-described embodiments, and various applications and modifications can be added to the scope of the invention in terms of the number of layers of the ceramic dielectric layer or the internal electrode constituting the ceramic laminate.

1‧‧‧積層陶瓷電容器 1‧‧‧Multilayer ceramic capacitors

2‧‧‧陶瓷介電層 2‧‧‧Ceramic dielectric layer

3、4‧‧‧內部電極 3, 4‧‧‧ internal electrodes

5‧‧‧陶瓷積層體 5‧‧‧Ceramic laminate

6、7‧‧‧外部電極 6, 7‧‧‧ external electrodes

L‧‧‧長度 L‧‧‧ length

T‧‧‧厚度 T‧‧‧ thickness

Claims (4)

一種積層陶瓷電容器,其特徵在於包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;且上述內部電極含有Ni與Sn,並且,上述內部電極之自與上述陶瓷介電層對向之表面起深度為20nm之區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上,且,上述內部電極之厚度方向之中央區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例未達40%。 A multilayer ceramic capacitor comprising: a ceramic layered body formed by laminating a plurality of ceramic dielectric layers; and a plurality of internal electrodes arranged to face each other with the ceramic dielectric layer interposed therebetween The inside of the ceramic laminate; and an external electrode disposed on the outer surface of the ceramic laminate in a manner to be electrically connected to the internal electrode; and the internal electrode includes Ni and Sn, and the internal electrode is self-contained The ratio of the ratio of Sn in the region of the surface of the ceramic dielectric layer facing the surface of the ceramic dielectric layer to the total amount of Sn and Ni, that is, the ratio of Sn/(Ni+Sn) to the ratio of 0.001 or more in terms of the molar ratio is 75% or more, and the ratio of Sn in the central region in the thickness direction of the internal electrode to the total amount of Sn and Ni, that is, the ratio of Sn/(Ni+Sn) to the region of 0.001 or more in terms of the molar ratio is not Up to 40%. 一種積層陶瓷電容器之製造方法,其特徵在於:其係用以製造如下積層陶瓷電容器之方法,該積層陶瓷電容器包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;且上述內部電極含有Ni與Sn,並且,上述內部電極之自與上述陶瓷介電層對向之表面起深度為20nm之區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比例為75%以上,且,上述內部電極之厚度方向之中央區域內之Sn相對於Sn與Ni之合計量之比即Sn/(Ni+Sn)比以莫耳比計為0.001以上的區域之比 例未達40%;上述積層陶瓷電容器之製造方法包括如下步驟:形成未煅燒陶瓷積層體,該未煅燒陶瓷積層體具有於積層並煅燒後成為上述陶瓷介電層之複數個未煅燒陶瓷介電層、及藉由塗佈導電膏而形成且沿著上述未煅燒陶瓷介電層間之複數個界面配設之複數個未煅燒內部電極圖案;以及藉由對上述未煅燒陶瓷積層體進行煅燒而獲得上述陶瓷積層體;並且,作為上述導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有與構成上述未煅燒陶瓷介電層之陶瓷材料粉末相同之組成或以其為基準之組成的陶瓷材料粉末中調配Sn成分而成。 A method for manufacturing a multilayer ceramic capacitor, characterized in that it is used for manufacturing a laminated ceramic capacitor comprising: a ceramic laminate comprising a plurality of ceramic dielectric layers; a plurality of internal electrodes And disposed in the ceramic laminate body so as to face each other with the ceramic dielectric layer interposed therebetween; and an external electrode disposed in the ceramic laminate body so as to be electrically connected to the internal electrode The outer surface; and the inner electrode includes Ni and Sn, and the ratio of Sn in the region of the inner electrode facing the ceramic dielectric layer to the surface of the ceramic dielectric layer having a depth of 20 nm with respect to the sum of Sn and Ni, that is, Sn The ratio of /(Ni+Sn) to the region of 0.001 or more in terms of the molar ratio is 75% or more, and the ratio of Sn in the central region in the thickness direction of the internal electrode to the total amount of Sn and Ni is Sn. Ratio of /(Ni+Sn) to an area of 0.001 or more in terms of molar ratio The method for manufacturing the multilayer ceramic capacitor includes the steps of: forming an uncalcined ceramic laminate having a plurality of uncalcined ceramic dielectrics which are laminated and calcined to form the ceramic dielectric layer. a layer and a plurality of uncalcined internal electrode patterns formed by coating a conductive paste and disposed along a plurality of interfaces between the uncalcined ceramic dielectric layers; and obtaining by calcining the uncalcined ceramic laminate The above-mentioned ceramic laminate; and, as the conductive paste, a conductive paste containing the same material as the Sn material, which is formulated to have the same composition as that of the ceramic material powder constituting the uncalcined ceramic dielectric layer, or It is prepared by blending a Sn component with a ceramic material powder having a reference composition. 一種積層陶瓷電容器,其特徵在於包括:陶瓷積層體,其係積層複數個陶瓷介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;且上述內部電極含有Ni與Sn,並且Sn固溶於Ni,上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例為2原子%以上,且,上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例較上述內部電極之自與上述陶瓷介電層之界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上。 A multilayer ceramic capacitor comprising: a ceramic layered body formed by laminating a plurality of ceramic dielectric layers; and a plurality of internal electrodes arranged to face each other with the ceramic dielectric layer interposed therebetween Inside the ceramic laminate; and an external electrode disposed on the outer surface of the ceramic laminate in a manner to be electrically connected to the internal electrode; and the internal electrode contains Ni and Sn, and Sn is dissolved in Ni, a ratio of Sn in a region having a depth of 2 nm from an interface with the ceramic dielectric layer to a total amount of Sn and Ni of 2 at% or more, and the internal electrode and the ceramic dielectric layer The ratio of Sn in the region having a depth of 2 nm to the total amount of Sn and Ni is larger than the ratio of Sn in the region of the internal electrode from the interface with the ceramic dielectric layer of 20 nm or more. %the above. 一種積層陶瓷電容器之製造方法,其特徵在於:該積層陶瓷電容器包括:陶瓷積層體,其係積層複數個陶瓷 介電層而成;複數個內部電極,其等係以介隔上述陶瓷介電層而互相對向之方式配設於上述陶瓷積層體之內部;及外部電極,其係以與上述內部電極導通之方式配設於上述陶瓷積層體之外表面;上述內部電極含有Ni與Sn,且Sn固溶於Ni;上述積層陶瓷電容器之製造方法包括如下步驟:形成未煅燒陶瓷積層體,該未煅燒陶瓷積層體具有於積層並煅燒後成為上述陶瓷介電層之複數個未煅燒陶瓷介電層、及藉由塗佈導電膏而形成且沿著上述未煅燒陶瓷介電層間之複數個界面配設之複數個未煅燒內部電極圖案;以及藉由對上述未煅燒陶瓷積層體進行煅燒而獲得上述陶瓷積層體;且作為上述導電膏,使用含有Sn成分調配相同材料之導電膏,該Sn成分調配相同材料係於具有含有構成陶瓷材料粉末之至少一部分元素之組成的陶瓷材料粉末中調配Sn成分而成,上述陶瓷材料粉末構成上述未煅燒陶瓷介電層,並且,以藉由對上述未煅燒陶瓷積層體進行煅燒而獲得上述陶瓷積層體之方式構成,上述陶瓷積層體係構成上述陶瓷積層體之上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例為2原子%以上,且上述內部電極之自與上述陶瓷介電層之界面起深度為2nm之區域內之Sn相對於Sn與Ni之合計量之比例較上述內部電極之自與上述陶瓷介電層之界面起深度為20nm以上之區域內之Sn之比例大1.0原子%以上。 A method of manufacturing a multilayer ceramic capacitor, characterized in that the multilayer ceramic capacitor comprises: a ceramic laminate, which is laminated with a plurality of ceramics a plurality of internal electrodes, which are disposed inside the ceramic laminate in such a manner as to face each other with the ceramic dielectric layer interposed therebetween; and an external electrode that is electrically connected to the internal electrode The method is disposed on the outer surface of the ceramic laminate; the internal electrode contains Ni and Sn, and Sn is dissolved in Ni; and the manufacturing method of the multilayer ceramic capacitor includes the following steps: forming an uncalcined ceramic laminate, the uncalcined ceramic The laminated body has a plurality of uncalcined ceramic dielectric layers which are laminated and calcined to form the ceramic dielectric layer, and are formed by applying a conductive paste and disposed along a plurality of interfaces between the uncalcined ceramic dielectric layers a plurality of uncalcined internal electrode patterns; and obtaining the ceramic laminate by calcining the unfired ceramic laminate; and as the conductive paste, using a conductive paste containing the same composition of the Sn component, the Sn component is formulated with the same material Forming a Sn material by mixing a ceramic material powder having a composition of at least a part of elements constituting the powder of the ceramic material, the ceramic The material powder constitutes the above-mentioned uncalcined ceramic dielectric layer, and is formed by calcining the above-mentioned uncalcined ceramic laminate to obtain the ceramic laminate, and the ceramic laminate system constitutes the internal electrode of the ceramic laminate a ratio of Sn to a total of Sn and Ni in a region having a depth of 2 nm from an interface of the ceramic dielectric layer is 2 atom% or more, and a depth of the internal electrode from an interface with the ceramic dielectric layer is The ratio of Sn in the region of 2 nm to the total amount of Sn and Ni is 1.0 atom% or more larger than the ratio of Sn in the region of the internal electrode from the interface with the ceramic dielectric layer to a depth of 20 nm or more.
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